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FDA 510(k)

SURFLO INJECTION PLUG

K-Number: K791173 · 1979-07-30

ApplicantTerumo America, Inc.
Decision Date1979-07-30
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SURFLO INJECTION PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Terumo America, Inc.. It received FDA 510(k) clearance on 1979-07-30 under 510(k) number K791173. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURFLO INJECTION PLUG?

SURFLO INJECTION PLUG is a medical device that received FDA 510(k) clearance on 1979-07-30. The listed applicant is Terumo America, Inc.. The 510(k) number is K791173.

When did SURFLO INJECTION PLUG receive FDA 510(k) clearance?

SURFLO INJECTION PLUG received FDA 510(k) clearance on 1979-07-30, under 510(k) number K791173.

Who is the listed applicant for SURFLO INJECTION PLUG?

The FDA 510(k) record lists Terumo America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURFLO INJECTION PLUG?

The FDA product code for SURFLO INJECTION PLUG is FPA.

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Other records listing Terumo America, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K811523PLASMA FLEXK802970TERUMO HOLLOW FIBER OXYGENATORK802122CLIRANS TH13 HOLLOW FIBER DIALYZERK802441CLIRANS TH10 HOLLOW FIBER DIALYZERK801194CLIRANS TE07 HOLLOW FIBER DIALYZERK801193CLIRANS TE15 HOLLOW FIBER DIALYZER

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Related Devices (Code: FPA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254123Ecomed Disposable Administration SetsEcomed Solutions, LLCK261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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